Parkinsonism in adult‐onset GM2 gangliosidosis
- 1 January 1994
- journal article
- research article
- Published by Wiley in Movement Disorders
- Vol. 9 (3) , 375-377
- https://doi.org/10.1002/mds.870090325
Abstract
No abstract availableKeywords
This publication has 16 references indexed in Scilit:
- Progressive dystonia symptomatic of juvenile GM2 gangliosidosisMovement Disorders, 1992
- The Clinical Aspects of Adult Hexosaminidase DeficienciesDevelopmental Neuroscience, 1991
- Molecular and Clinical Heterogeneity of Adult GM2 GangliosidosisDevelopmental Neuroscience, 1991
- Neuropathology of Late Onset GangliosidosesDevelopmental Neuroscience, 1991
- An adult onset hexosaminidase A deficiency syndrome with sensory neuropathy and internuclear ophthalmoplegia.Journal of Neurology, Neurosurgery & Psychiatry, 1991
- Hexosaminidase A deficiency in adultsAmerican Journal of Medical Genetics, 1986
- Movement Disorders Associated with Chronic GM2 GangliosidosisEuropean Neurology, 1986
- Motor neuron disease and adult hexosaminidase a deficiency in two families: Evidence for multisystem degenerationAnnals of Neurology, 1985
- Juvenile progressive dystonia: A new phenotype of GM2 GangliosidosisAnnals of Neurology, 1984
- GM2-gangliosidosis Hexosaminidase mutations not of the Tay-Sachs type procedure unusual clinical variantsTrends in Neurosciences, 1983